Evidence map›Paper›PMID 42723752›Full record

ArticleTranslational lung cancer research2026

Association of FDG PET/CT and immune profiling with pathologic complete response after neoadjuvant immunotherapy in stage II-III non-small cell lung cancer.

Eun Seong Lee, Saem Mul Park, Seunghun Lee, Sehui Kim, Juwhan Choi, Jun Hee Lee, Jae Seon Eo, Hyun Koo Kim, Hwan Seok Yong, Chun-Jen J Chen and 3 more

Abstract read
In one paragraph

Article in Translational lung cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Eun Seong Lee *Department of Nuclear Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Saem Mul Park *School of Biological Sciences, The University of Auckland, Auckland, New Zealand.
Seunghun LeeDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Sehui KimDepartment of Pathology, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Juwhan ChoiDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Jun Hee LeeDepartment of Thoracic and Cardiovascular Surgery, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Jae Seon EoDepartment of Nuclear Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Hyun Koo KimDepartment of Thoracic and Cardiovascular Surgery, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Hwan Seok YongDepartment of Radiology, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Chun-Jen J ChenSchool of Biological Sciences, The University of Auckland, Auckland, New Zealand.
Heidi RobinsonSchool of Biological Sciences, The University of Auckland, Auckland, New Zealand.
P Rod Dunbar *School of Biological Sciences, The University of Auckland, Auckland, New Zealand.
Sung Yong Lee *Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neoadjuvant immunotherapy has emerged as a transformative approach for resectable non-small cell lung cancer (NSCLC). Pathologic complete response (pCR) after neoadjuvant therapy serves as a robust surrogate marker for early treatment efficacy and long-term outcomes. However, reliable noninvasive predictors of pCR before surgery remain an unmet clinical need. This study investigated the association between fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) parameters and tumor-infiltrating immune cell subsets in pre-treatment biopsies with pCR in patients with stage II-III NSCLC treated with immune checkpoint inhibitor (ICI)-based neoadjuvant therapy. Methods: We retrospectively analyzed 13 patients with stage II-III NSCLC who underwent ICI-based neoadjuvant therapy and baseline FDG PET/CT. pCR was assessed in resected surgical specimens. PET/CT parameters, including tumor-to-liver ratio (TLR) and maximum standardized uptake value (SUVmax), were evaluated before and after neoadjuvant treatment. Multiplex immunofluorescence (mIF) was performed on pre-treatment tumor biopsies to quantify tumor-infiltrating immune cell subsets and functional immune markers. Results: Eight patients (62%) achieved pCR. Compared with the non-pCR group, patients with pCR showed significantly lower post-treatment TLR (median 1.51 Conclusions: Dynamic changes in PET/CT-derived TLR and immune biomarkers from pre-treatment biopsies were associated with pCR following neoadjuvant immunotherapy in stage II-III NSCLC. These findings support the complementary role of metabolic imaging and immune profiling in improving patient selection and perioperative decision-making.

Indexed as

Fluorodeoxyglucose positron emission tomography/computed tomography (FDG PET/CT)immune biomarkersneoadjuvant immunotherapynon-small cell lung cancer (NSCLC)pathologic complete response (pCR)

Identifiers

PMID42723752
PMCPMC13557881

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.